Lunar tungsten isotopic evidence for the late veneer.

According to the most widely accepted theory of lunar origin, a giant impact on the Earth led to the formation of the Moon, and also initiated the final stage of the formation of the Earth's core. Core formation should have removed the highly siderophile elements (HSE) from Earth's primitive mantle (that is, the bulk silicate Earth), yet HSE abundances are higher than expected. One explanation for this overabundance is that a 'late veneer' of primitive material was added to the bulk silicate Earth after the core formed. To test this hypothesis, tungsten isotopes are useful for two reasons: first, because the late veneer material had a different (182)W/(184)W ratio to that of the bulk silicate Earth, and second, proportionally more material was added to the Earth than to the Moon. Thus, if a late veneer did occur, the bulk silicate Earth and the Moon must have different (182)W/(184)W ratios. Moreover, the Moon-forming impact would also have created (182)W differences because the mantle and core material of the impactor with distinct (182)W/(184)W would have mixed with the proto-Earth during the giant impact. However the (182)W/(184)W of the Moon has not been determined precisely enough to identify signatures of a late veneer or the giant impact. Here, using more-precise measurement techniques, we show that the Moon exhibits a (182)W excess of 27 ± 4 parts per million over the present-day bulk silicate Earth. This excess is consistent with the expected (182)W difference resulting from a late veneer with a total mass and composition inferred from HSE systematics. Thus, our data independently show that HSE abundances in the bulk silicate Earth were established after the giant impact and core formation, as predicted by the late veneer hypothesis. But, unexpectedly, we find that before the late veneer, no (182)W anomaly existed between the bulk silicate Earth and the Moon, even though one should have arisen through the giant impact. The origin of the homogeneous (182)W of the pre-late-veneer bulk silicate Earth and the Moon is enigmatic and constitutes a challenge to current models of lunar origin.

The 146 Sm half-life re-measured: consolidating the chronometer for events in the early Solar System.

The half-life of the extinct radiolanthanide 146 Sm , important for both geochronological and astrophysical applications, was re-determined by a combination of mass spectrometry and α -decay counting. Earlier studies provided only limited information on all potential factors that could influence the quantification of the half-life of 146 Sm . Thus, special attention was given  here to a complete documentation of all experimental steps to provide information about any possible artifacts in the data analysis. The half-life of 146 Sm was derived to be 92.0 Ma ± 2.6 Ma, with an uncertainty coverage factor of k = 1 .

Determination of the half-life of gadolinium-148.

The half-life of the alpha-emitter 148Gd was measured using the "direct method", in which the number of atoms is directly determined and their activity is then measured. Pure Gd samples containing megabecquerels of 148Gd were obtained by reprocessing proton-irradiated tantalum material. Multicollector-inductively coupled plasma mass spectrometry was performed to determine the amount of 148Gd atoms retrieved. The activity of the 148Gd atoms contained in the Gd sample was measured by means of alpha-spectrometry. The half-life of 148Gd was deduced to be 86.9 years, with a combined uncertainty of 4.5%.

High precision half-life measurement of the extinct radio-lanthanide Dysprosium-154.

Sixty years after the discovery of 154Dy, the half-life of this pure alpha-emitter was re-measured. 154Dy was radiochemically separated from proton-irradiated tantalum samples. Sector field- and multicollector-inductively coupled plasma mass spectrometry were used to determine the amount of 154Dy retrieved. The disintegration rate of the radio-lanthanide was measured by means of α-spectrometry. The half-life value was determined as (1.40 ± 0.08)∙106 y, with an uncertainty reduced by a factor of ~ 10 compared to the currently adopted value of (3.0 ± 1.5)∙106 y. This precise half-life value is useful for the the correct testing and evaluation of p-process nucleosynthetic models using 154Dy as a seed nucleus or as a reaction product, as well as for the safe disposal of irradiated target material from accelerator driven facilities. As a first application of the half-life value determined in this work, the excitation functions for the production of 154Dy in proton-irradiated Ta, Pb, and W targets were re-evaluated, which are now in agreement with theoretical calculations.

Efficient Production of High Specific Activity Thulium-167 at Paul Scherrer Institute and CERN-MEDICIS.

Thulium-167 is a promising radionuclide for nuclear medicine applications with potential use for both diagnosis and therapy ("theragnostics") in disseminated tumor cells and small metastases, due to suitable gamma-line as well as conversion/Auger electron energies. However, adequate delivery methods are yet to be developed and accompanying radiobiological effects to be investigated, demanding the availability of 167Tm in appropriate activities and quality. We report herein on the production of radionuclidically pure 167Tm from proton-irradiated natural erbium oxide targets at a cyclotron and subsequent ion beam mass separation at the CERN-MEDICIS facility, with a particular focus on the process efficiency. Development of the mass separation process with studies on stable 169Tm yielded 65 and 60% for pure and erbium-excess samples. An enhancement factor of thulium ion beam over that of erbium of up to several 104 was shown by utilizing laser resonance ionization and exploiting differences in their vapor pressures. Three 167Tm samples produced at the IP2 irradiation station, receiving 22.8 MeV protons from Injector II at Paul Scherrer Institute (PSI), were mass separated with collected radionuclide efficiencies between 11 and 20%. Ion beam sputtering from the collection foils was identified as a limiting factor. In-situ gamma-measurements showed that up to 45% separation efficiency could be fully collected if these limits are overcome. Comparative analyses show possible neighboring mass suppression factors of more than 1,000, and overall 167Tm/Er purity increase in the same range. Both the actual achieved collection and separation efficiencies present the highest values for the mass separation of external radionuclide sources at MEDICIS to date.